{"id":21134,"date":"2025-11-17T01:45:42","date_gmt":"2025-11-16T22:45:42","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/williams\/"},"modified":"2025-11-17T01:45:42","modified_gmt":"2025-11-16T22:45:42","slug":"williams-sendromu","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/williams-sendromu\/","title":{"rendered":"Williams Syndrome"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Williams syndrome is a genetic disorder characterized by an elfin face, cardiovascular anomalies, and developmental delay.<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Elfin face<\/li>\n<li>Supravular aortic stenosis<\/li>\n<li>Hypercalcemia<\/li>\n<li>Developmental delay<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>Chromosome 7 deletion.<\/p>\n<h2>Diagnosis<\/h2>\n<p>Genetic testing.<\/p>\n<h2>Treatment<\/h2>\n<p>Symptomatic treatment.<\/p>\n<h2>Which Polyclinic Should You Apply To?<\/h2>\n<p><strong>Genetics Polyclinic<\/strong><\/p>\n<h2>What to Do in an Emergency?<\/h2>\n<p>In case of symptoms of heart failure, emergency services should be sought.<\/p>\n<p><em>This page is for general information purposes only.<\/em><\/p>","protected":false},"excerpt":{"rendered":"<p>Definition Williams syndrome is a genetic disorder characterized by elf-like facial features, cardiovascular abnormalities, and developmental delay. Symptoms Elfin facial features Supravlvular aortic stenosis Hypercalcemia Developmental delay Causes Deletion of chromosome 7. Diagnosis Genetic testing. Treatment Symptomatic treatment. Which Clinic Should You Go To? Genetics Clinic What to Do in an Emergency? In case of symptoms of heart failure, go to the emergency room. This page is for general information purposes only [\u2026]<\/p>","protected":false},"author":1,"featured_media":0,"menu_order":0,"template":"","format":"standard","meta":{"_acf_changed":false,"slim_seo":{"title":"Williams Syndrome - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition Williams syndrome is a genetic disorder characterized by elfin facial features, cardiovascular abnormalities, and developmental delay. Symptoms Elfin facial features Supravvulcular"},"footnotes":""},"class_list":["post-21134","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21134","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar"}],"about":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/types\/hastaliklar"}],"author":[{"embeddable":true,"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/users\/1"}],"version-history":[{"count":1,"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21134\/revisions"}],"predecessor-version":[{"id":21170,"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21134\/revisions\/21170"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21134"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}